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Duolock

FDA UDI

Class I (US FDA UDI)

by Convatec, Purchasing Department

Identity

Trade Name
DUOLOCK FDA UDI
Generic Name
Ostomy bag closure device FDA UDI
Device Name
Duolock® Curved Tail Closures FDA UDI
Model / Reference
175652 FDA UDI
Description
Duolock® Curved Tail Closures FDA UDI

Identifiers

Primary DI / UDI-DI
00768455108671 FDA UDI
FDA Product Code
EZS FDA UDI
GMDN Term
Ostomy bag closure device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ostomy bag closure device

Duolock by Convatec, Purchasing Department — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ostomy bag closure device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c4c75fc7-a346-4d7e-b2a8-6abc15a83e84 34 fields · synced May 30, 2026